terbutaline sulfate

Generic: terbutaline sulfate

Labeler: chartwell rx, llc.
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name terbutaline sulfate
Generic Name terbutaline sulfate
Labeler chartwell rx, llc.
Dosage Form TABLET
Routes
ORAL
Active Ingredients

terbutaline sulfate 5 mg/1

Manufacturer
Chartwell RX, LLC.

Identifiers & Regulatory

Product NDC 62135-525
Product ID 62135-525_459ef32e-2348-14bd-e063-6394a90a6a90
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA077152
Listing Expiration 2026-12-31
Marketing Start 2005-03-25

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 62135525
Hyphenated Format 62135-525

Supplemental Identifiers

RxCUI
857677 857683
UPC
0362135524906 0362135525903
UNII
576PU70Y8E

Packaging Origin

Original Packager
true

Resolved Product View

Precedence rule: structured NDC data is preferred, falling back to linked label metadata when unavailable. Source tags show the origin of each value.

Resolved Identity

Brand Name terbutaline sulfate (source: ndc)
Generic Name terbutaline sulfate (source: ndc)
Application Number ANDA077152 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 5 mg/1
source: ndc
Packaging
  • 90 TABLET in 1 BOTTLE (62135-525-90)
source: ndc

Packages (1)

Ingredients (1)

terbutaline sulfate (5 mg/1)

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "459ef32e-2348-14bd-e063-6394a90a6a90", "openfda": {"upc": ["0362135524906", "0362135525903"], "unii": ["576PU70Y8E"], "rxcui": ["857677", "857683"], "spl_set_id": ["859267c6-3d14-4123-9b9d-4fc248f09726"], "manufacturer_name": ["Chartwell RX, LLC."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "90 TABLET in 1 BOTTLE (62135-525-90)", "package_ndc": "62135-525-90", "marketing_start_date": "20230228"}], "brand_name": "Terbutaline Sulfate", "product_id": "62135-525_459ef32e-2348-14bd-e063-6394a90a6a90", "dosage_form": "TABLET", "product_ndc": "62135-525", "generic_name": "Terbutaline Sulfate", "labeler_name": "Chartwell RX, LLC.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Terbutaline Sulfate", "active_ingredients": [{"name": "TERBUTALINE SULFATE", "strength": "5 mg/1"}], "application_number": "ANDA077152", "marketing_category": "ANDA", "marketing_start_date": "20050325", "listing_expiration_date": "20261231"}